Variant #0000274532 (NC_000016.9:g.67645876_67645877del, NM_006565.3:c.804_805del (CTCF))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.67645876_67645877del |
| DNA change (hg38) |
g.67611973_67611974del |
| Published as |
CTCF(NM_006565.3):c.804_805delTG (p.C268*) |
| ISCN |
- |
| DB-ID |
CTCF_000004 |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2020-07-09 17:57:23 +02:00 (CEST) |

Variant on transcripts
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